A First‑in‑Human Phase 1 Study to Investigate the Safety, Tolerability, and PK of AB102 in Healthy Participants

2026-526279-52-00 Protocol ARC-102-101 Human pharmacology (Phase I) - First administration to humans Authorised, recruiting

Start 26 Jun 2026 · Status Authorised, recruiting · 1 EU/EEA countries · 1 sites · Protocol ARC-102-101

Overview

Sponsor-declared trial summary

Phase Human pharmacology (Phase I) - First administration to humans
Status Authorised, recruiting
Participants planned 130
Countries 1
Sites 1

Healthy volunteers

Key facts

Sponsor
Arcus Biosciences Inc.
Participant type
Healthy volunteers
Age range
18-64 years
Gender
Male and Female
Therapeutic area
Diseases [C] - Skin and Connective Tissue Diseases [C17]
Trial duration
26 Jun 2026 → ongoing
Decision date (initial)
2026-06-16
Transition trial
No
Low-intervention
No
Rare-disease indication
No
Vulnerable population
Yes

Trial design

CTIS Part I — objectives, methods, condition coding

Conditions and MedDRA coding

Healthy volunteers

Sponsors and contacts

Sponsor organisations, regulatory contacts, third parties

Arcus Biosciences Inc.

Sponsor organisation
Arcus Biosciences Inc.
Address
3928 Point Eden Way
City
Hayward
Postcode
94545-3719
Country
United States

Scientific contact point

Organisation
Arcus Biosciences Inc.
Contact name
Medical Director

Public contact point

Organisation
Arcus Biosciences Inc.
Contact name
Medical Director

Locations

1 EU/EEA country · 1 investigational sites

By country

CountryMS statusPlanned subjectsSites
Netherlands Authorised, recruiting 130 1
Rest of world 0

Investigational sites

Netherlands

1 site · Authorised, recruiting
Pharmaceutical Research Associates Group B.V.
Program Management, Van Swietenlaan 6, 9728 NZ, Groningen

Country notifications

Trial-start, recruitment-start, end and early-termination notifications submitted per Member State

Country Trial startTrial end Recruitment startRecruitment end Early termination
Netherlands 2026-06-26

Application history

1 submissions — initial application plus substantial / non-substantial modifications

#TypeCodeSubmittedReference MSConclusionDecision date
1 INITIAL IN 2026-05-04 Netherlands Acceptable
2026-06-16
2026-06-16